Construction and characterization of a one-plasmid system for the controlled expression of genes in mammalian cells by tetracycline

被引:20
作者
OBrien, K
Otto, K
Rao, RN
机构
[1] Cancer Research, Lilly Research Laboratories, A Division of Eli Lilly and Company, Indianapolis
关键词
cloning; tetR; VP16; p53; raf; hygromycin; transformed phenotype; stable transfection;
D O I
10.1016/S0378-1119(96)00583-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The two-plasmid system of Gossen and Bujard [Gossen and Bujard (1992) Proc. Natl. Acad. Sci. USA 89, 5547-5551] to express mammalian genes in a tetracycline-repressed fashion was combined into a single-plasmid system. Two variants of this single-plasmid system that differ in the multiple cloning site (MCS) region are described. These vectors were used to stably transfect raf kinase domain into the normal rat kidney epithelial cell line (NRKE) to obtain a conditionally transformed cell line. These vectors were also used to stably transfect wild-type and mutant human p53 into the human osteosarcoma cell line, SAOS-2. Tetracycline repressed gene expression in both cell lines; about 12-fold in NRKE and about SO-fold in SAOS-2 cell line.
引用
收藏
页码:115 / 120
页数:6
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